ENST00000585465.3:c.*2802A>C
|
ENSP00000490268.2:n.*2802A>C
|
|
ENST00000585748.3:c.829A>C
|
ENSP00000477641.2:p.Ser277Arg
|
|
ENST00000585851.2:c.1027A>C
|
ENSP00000467912.2:p.Ser343Arg
|
|
ENST00000326873.12:c.1201A>C
MANE Select
|
ENSP00000324856.6:p.Ser401Arg
|
|
ENST00000326873.11:c.1201A>C
|
ENSP00000324856.6:p.Ser401Arg
|
|
ENST00000585465.2:n.2934A>C
|
|
|
ENST00000586243.5:c.1201A>C
|
ENSP00000467240.2:p.Ser401Arg
|
|
ENST00000589152.5:n.1899A>C
|
|
|
NM_000455.4:c.1201A>C , LRG_319t1:c.1201A>C
|
NP_000446.1:p.Ser401Arg
|
|
XM_005259617.1:c.1196A>C
|
XP_005259674.1:p.Glu399Ala
|
|
XM_011528209.1:c.974A>C
|
XP_011526511.1:p.Glu325Ala
|
|
XM_005259617.3:c.1196A>C
|
XP_005259674.1:p.Glu399Ala
|
|
XM_011528209.2:c.974A>C
|
XP_011526511.1:p.Glu325Ala
|
|
XR_001753738.2:n.2007A>C
|
|
|
XR_001753740.2:n.1977A>C
|
|
|
NM_000455.5:c.1201A>C
MANE Select
|
NP_000446.1:p.Ser401Arg
|
|